Glycerol 3-phosphate dehydrogenase for butanol production

US9944954B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9944954-B2
Application numberUS-201615228770-A
CountryUS
Kind codeB2
Filing dateAug 4, 2016
Priority dateMar 14, 2013
Publication dateApr 17, 2018
Grant dateApr 17, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Provided herein are glycerol-3-phosphate dehydrogenase (GPD) enzymes with increased K M for NADH and GPD enzymes with substantially the same affinity for NADH and NADPH and/or are feedback inhibited by glycerol-3-phosphate. Also provided herein are recombinant microorganisms comprising a heterologous gene encoding GPD and a deletion or disruption in an endogenous gene encoding GPD. Also provided are recombinant microorganisms comprising a heterologous gene encoding GPD and a butanol biosynthetic pathway. Further provided are methods of producing butanol comprising providing the recombinant microorganisms described herein and contacting the recombinant microorganism with at least one fermentable carbon substrate under conditions wherein butanol is produced.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for the production of isobutanol comprising: (a) providing a recombinant microorganism comprising i. an engineered isobutanol biosynthetic pathway, ii. a deletion or disruption in an endogenous gene encoding GPD1, and iii. an engineered glycerol-3-phosphate dehydrogenase (GPD) enzyme wherein the GPD has at least 90% identity to SEQ ID NO: 195 and comprises at least one substitution at a residue corresponding to position 44, 45, 73, or 129 of SEQ ID NO: 195, and wherein the engineered GPD has a higher K M for NADH as compared to the K M of the endogenous GPD of the microorganism; and (a) contacting the recombinant microorganism with at least one fermentable carbon substrate under conditions wherein isobutanol is produced. 2. The method of claim 1 , wherein the recombinant microorganism is grown under anaerobic conditions. 3. The method of claim 1 , wherein the enzyme comprises at least one substitution corresponding to position 73 of SEQ ID NO: 195. 4. The method of claim 1 , wherein the enzyme comprises at least one substitution corresponding to position 129 of SEQ ID NO:195. 5. The method of claim 1 , wherein the enzyme comprises a substitution corresponding to position 73 of SEQ ID NO:195 and a substitution corresponding to position 129 of SEQ ID NO:195. 6. The method of claim 1 , wherein the isobutanol biosynthetic pathway comprises at least one gene encoding a polypeptide that performs at least one of the following substrate to product conversions: (a) pyruvate to acetolactate, as catalyzed by acetolactate synthase; (b) acetolactate to 2,3-dihydroxyisovalerate, as catalyzed by acetohydroxy acid isomeroreductase; (c) 2,3-dihydroxyisovalerate to α-ketoisovalerate, as catalyzed by dihydroxyacid dehydratase; (d) α-ketoisovalerate to isobutyraldehyde, as catalyzed by a branched chain keto acid decarboxylase; and (e) isobutyraldehyde to isobutanol, as catalyzed by branched-chain alcohol dehydrogenase. 7. The method of claim 1 , wherein the microorganism is from a genus selected from the group consisting of Clostridium, Zymomonas, Escherichia, Salmonella, Serratia, Envinia, Klebsiella, Shigella, Rhodococcus, Pseudomonas, Bacillus, Lactobacillus, Enterococcus, Alcaligenes, Paenibacillus, Arthrobacter, Corynebacterium, Brevibacterium, Schizosaccharomyces, Kluveromyces, Yarrowia, Pichia, Zygosaccharomyces, Debaryomyces, Candida, Brettanomyces, Pachysolen, Hansenula, Issatchenkia, Trichosporon Yamadazyma, and Saccharomyces. 8. The method of claim 7 , wherein the microorganism is from the genus Saccharomyces. 9. The method of claim 1 , wherein the microorganism comprises a ketol-acid reductoisomerase (KARI) that utilizes NADH. 10. The method of claim 1 , further comprising recovering the isobutanol. 11. The method of claim 10 , wherein the isobutanol is recovered by distillation, azeotropic distillation, liquid-liquid extraction, adsorption, gas stripping, membrane evaporation, pervaporation, or combinations thereof.

Assignees

Inventors

Classifications

  • Glycerol-3-phosphate dehydrogenase (NAD+) (1.1.1.8) · CPC title

  • Genes encoding for enzymes or proenzymes · CPC title

  • acting on CH-OH groups as donors (1.1) · CPC title

  • Glycerol-3-phosphate dehydrogenase (NAD(P)+)(1.1.1.94) · CPC title

  • Glyceraldehyde-3-phosphate dehydrogenase (phosphorylating) (1.2.1.12) · CPC title

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What does patent US9944954B2 cover?
Provided herein are glycerol-3-phosphate dehydrogenase (GPD) enzymes with increased K M for NADH and GPD enzymes with substantially the same affinity for NADH and NADPH and/or are feedback inhibited by glycerol-3-phosphate. Also provided herein are recombinant microorganisms comprising a heterologous gene encoding GPD and a deletion or disruption in an endogenous gene encoding GPD. Also provid…
Who is the assignee on this patent?
Butamax Advanced Biofuels Llc
What technology area does this patent fall under?
Primary CPC classification C12P7/16. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).